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Z-0876-2026Class II

Microbiologics Inc

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Microbiologics Inc
Product type
Device
Status
Ongoing
Report date
2025-12-10
Distribution
International distribution to the countries of UAE, China, Singapore, Kazakhstan,
Firm state
MN
Product quantity
5 units
Initiated by
Voluntary: Firm initiated
Reason for recall

Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.

Product description

KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K

Code / lot info

UDI-DI: 30845357020018; Lot Number: 818-111-7

Other recalls SPEQ maps to Documentation & Change Control
See all Documentation & Change Control recalls →

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →